Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Universal STAR-T Cell Injection is an allogeneic (off-the-shelf) cell therapy being developed for the treatment of multiple sclerosis (MS), including progressive and relapsing-remitting forms. The therapy utilizes Synthetic T-cell Antigen Receptor (STAR) technology, which involves engineering T cells to express a synthetic receptor that fuses antibody-derived antigen-recognition domains with the constant regions of a natural T-cell receptor (TCR). This design is intended to provide more physiological signaling and higher sensitivity than traditional Chimeric Antigen Receptors (CARs). The "universal" aspect of the therapy indicates that the cells are derived from healthy donors and gene-edited to prevent graft-versus-host disease (GvHD) and rejection by the recipient's immune system, allowing for immediate use without patient-specific manufacturing. The therapy targets B-cell populations (specifically CD19) to eliminate the cells responsible for the autoimmune response in MS. It is currently in Phase I clinical development under the leadership of Daishi Tian at Tianjin Medical University.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Universal STAR-T Cell Injection.